| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:44139395-44139563 | Common:3; Rare:42 | ||||
| chr6:44176432-44176615 | Rare:55 | ||||
| chr6:44246875-44247192 | Common:4; Rare:133 | ||||
| chr6:46129803-46129993 | Common:3; Rare:47 | ||||
| chr6:46652655-46653105 | Common:1; Rare:113 | ||||
| chr6:46921913-46922076 | Rare:43 | ||||
| chr6:47477695-47478073 | Common:3; Rare:93; Clinvar:5; Clinvar (benign):4 | ||||
| chr6:47478075-47478243 | Common:1; Rare:65; Clinvar:2; Clinvar (benign):2 | ||||
| chr6:49463137-49463407 | Common:1; Rare:75; Clinvar:2; Clinvar (benign):1 | ||||
| chr6:52576987-52577292 | Common:5; Rare:114 | ||||
| chr6:52671009-52671175 | Rare:51 | ||||
| chr6:52909651-52909736 | Common:2; Rare:22 | ||||
| chr6:52995249-52995832 | Common:4; Rare:234 | ||||
| chr6:53061620-53061926 | Rare:69 | ||||
| chr6:53065369-53065604 | Common:1; Rare:72 |